MeSH Browser

MeSH Heading: Acatalasia
Tree Number(s): C16.320.565.663.050; C18.452.648.663.050
Unique ID: D020642
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D020642
Scope Note: A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present.
Entry Term(s): Acatalasemia; Acatalasemia Japanese Type; Acatalasemia Swiss Type; Catalase Deficiency; Hypocatalasemia; Hypocatalasia; Takahara Disease; Takahara's Disease
Previous Indexing: Catalase (1965-1999)
Public MeSH Note: 2000
History Note: 2000
Date Established: 2000/01/01
Date of Entry: 1999/11/03
Revision Date: 2015/06/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0328366
Scope Note: A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present.
Terms: Acatalasia Preferred Term
Term UI T358366
Date10/12/1999
LexicalTag NON
ThesaurusID; Takahara Disease
Term UI T364492
Date10/12/1999
LexicalTag EPO
ThesaurusID NLM (2000); Takahara's Disease
Term UI T364493
Date10/12/1999
LexicalTag EPO
ThesaurusID NLM (2000); Acatalasemia
Term UI T364494
Date10/12/1999
LexicalTag NON
ThesaurusID

Acatalasia MeSH Descriptor Data 2024